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Stock impact report

Protalix BioTherapeutics advances Fabry disease and gout programs during 2025 [Yahoo! Finance]

Protalix BioTherapeutics, Inc. (DE) (PLX) 
Company Research Source: Yahoo! Finance
Protalix Biotherapeutics Inc (NYSE-A:PLX, FRA:PBDA) reported its 2025 financial results and outlined recent regulatory, clinical and commercial developments, including a new European approval for its Fabry disease therapy and updated guidance for 2026. "2025 was a year of meaningful progress for Protalix, marked by strong commercial execution with our partners and important advances and strategic direction across our clinical and preclinical pipeline," the company's CEO Dror Bashan said. "The EC approval of the E4W dosing regimen for Elfabrio in the European Union represents an advancement for patients by reducing treatment burden without compromising efficacy. This milestone strengthens the long–term value of our Fabry franchise.” The European Commission approved a 2 mg/kg every-four-weeks dosing regimen for Elfabrio in adults with Fabry disease who are stable on enzyme replacement therapy. The company said the less frequent dosing schedule reduces treatment burden while mai Show less Read more
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